Process Engineer

Yoh,-A-Day-; Noblesville (IN); On-site; USD 95,000 - 110,000; Full time

Benefits offered by this job

Medical benefits

Dental & Vision benefits

HSA

Life Insurance

Disability Insurance

401K

Direct Deposit

Referral bonuses

Training opportunities

Job summary

Yoh is seeking a Process Engineer for a pharmaceutical manufacturing client in Noblesville, Indiana. The role supports a fast-paced sterile drug-product operation and leads process and equipment improvements in a cGMP environment.

Responsibilities include establishing KPIs, troubleshooting, root-cause investigations, change controls, and working cross-functionally with Quality, Manufacturing, Validation, and R&D to ensure compliant implementation and successful product launches.

Qualifications

• Five or more years of relevant engineering experience in a cGMP manufacturing environment.
• Hands-on experience troubleshooting manufacturing processes or equipment and implementing sustainable reliability or quality improvements.
• Experience leading formal root-cause analysis using structured problem-solving methodologies.
• Experience authoring deviations, CAPAs, change controls, protocols, technical reports, or comparable controlled documentation.
• Working knowledge of cGMP requirements, validation, quality systems, document control, and the regulatory impact of engineering changes.

Responsibilities

• Lead process improvement, equipment reliability, troubleshooting, and remediation initiatives across manufacturing operations.
• Establish and monitor process KPIs related to reliability, quality, throughput, yield, downtime, and operational performance.
• Evaluate, design, and implement robust manufacturing processes for new products using existing or new equipment.
• Support product launches, technology transfers, and implementation of new manufacturing lines.
• Lead formal root-cause investigations involving manufacturing processes and equipment.
• Author deviations, determine root causes, and develop corrective and preventive actions to prevent recurrence.
• Write and execute technical documentation, including engineering protocols, reports, risk assessments, and process-improvement documentation.
• Initiate and support change controls associated with equipment and process improvements.
• Partner with Quality, Manufacturing, Validation, Technical Services, R&D, and other functions to ensure compliant implementation of cGMP practices.
• Provide input into project-cost forecasts and track project activities against established milestones.
• Develop and maintain manufacturing procedures, batch records, equipment documentation, and training materials.
• Provide hands-on manufacturing-floor support during equipment issues, process changes, startup activities, and project implementation.

Skills

Project management

Organizational skills

Technical writing

Communication

Education

Bachelor's degree in Engineering

Job description

Yoh is hiring a Process Engineer for our Pharmaceutical Manufacturing client in Noblesville, Indiana. This position will support a fast-paced sterile drug-product manufacturing operation. The Process Engineer will lead process and equipment improvements, troubleshoot manufacturing issues, establish performance metrics, investigate failures, and support new products and manufacturing lines within a cGMP environment.

What You Will Do

• Lead process improvement, equipment reliability, troubleshooting, and remediation initiatives across manufacturing operations.
• Establish and monitor process KPIs related to reliability, quality, throughput, yield, downtime, and operational performance.
• Evaluate, design, and implement robust manufacturing processes for new products using existing or new equipment.
• Support product launches, technology transfers, and implementation of new manufacturing lines.
• Lead formal root-cause investigations involving manufacturing processes and equipment.
• Author deviations, determine root causes, and develop corrective and preventive actions to prevent recurrence.
• Write and execute technical documentation, including engineering protocols, reports, risk assessments, and process-improvement documentation.
• Initiate and support change controls associated with equipment and process improvements.
• Partner with Quality, Manufacturing, Validation, Technical Services, R&D, and other functions to ensure compliant implementation of cGMP practices.
• Provide input into project-cost forecasts and track project activities against established milestones.
• Develop and maintain manufacturing procedures, batch records, equipment documentation, and training materials.
• Provide hands‑on manufacturing‑floor support during equipment issues, process changes, startup activities, and project implementation.

Education and Experience Requirements

• Bachelor’s degree in Engineering required. Mechanical Engineering is preferred; Chemical, Biochemical, Biotechnology, Manufacturing, or another engineering discipline may be considered based on relevant experience.
• Five or more years of relevant engineering experience in a cGMP manufacturing environment.
• Demonstrated experience optimizing manufacturing processes and establishing or monitoring process KPIs.
• Hands‑on experience troubleshooting manufacturing processes or equipment and implementing sustainable reliability or quality improvements.
• Experience leading formal root‑cause analysis using structured problem‑solving methodologies.
• Experience authoring deviations, CAPAs, change controls, protocols, technical reports, or comparable controlled documentation.
• Working knowledge of cGMP requirements, validation, quality systems, document control, and the regulatory impact of engineering changes.
• Experience supporting cross‑functional projects from evaluation and design through implementation and operational handoff.
• Strong project‑management, organizational, technical‑writing, and communication skills.
• Ability to work independently while collaborating effectively within multidisciplinary project and manufacturing teams.

Preferred Experience

• Automated visual inspection systems
• Vial inspection or vial‑labeling equipment
• Pharmaceutical packaging equipment or packaging lines
• Sterile injectable, aseptic, or fill‑finish manufacturing
• New‑product introduction, technology transfer, or manufacturing‑line startup
• Medical‑device or other highly regulated manufacturing environments may also be considered when accompanied by strong process‑engineering, validation, and quality‑system experience

Additional Requirements

• Must be able to work fully onsite in Noblesville, Indiana, Monday through Friday from 8:00 a.m.–5:00 p.m.

#IND-SPG

Estimated Min Rate

$95000.00

Estimated Max Rate

$110000.00

What’s In It for You?

We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

• Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
• Health Savings Account (HSA) (for employees working 20+ hours per week)
• Life & Disability Insurance (for employees working 20+ hours per week)
• MetLife Voluntary Benefits
• Employee Assistance Program (EAP)
• 401K Retirement Savings Plan
• Direct Deposit & weekly epayroll
• Referral Bonus Programs
• Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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